Canonical Allele Identifier: CA248845

Gene: MT-ND6

Linked Data

• ClinVar Variation Id: 218344
• ClinVar RCV Id: RCV000202587
• dbSNP Id: rs1556424431
• MyVariant Identifiers: chrMT:g.14372C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14372C>A , J01415.2:m.14372C>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361681.2:c.302G>T	ENSP00000354665.2:p.Gly101Val